Department of Molecular Science and Nanosystems, Ca' Foscari University of Venice, Via Torino 155, I-30172 Venezia Mestre, Italy.
Department of Molecular Science and Nanosystems, Ca' Foscari University of Venice, Via Torino 155, I-30172 Venezia Mestre, Italy.
Talanta. 2017 Sep 1;172:133-138. doi: 10.1016/j.talanta.2017.05.039. Epub 2017 May 14.
In this paper we present an electrochemical approach to prepare standard solutions of metal ions in a room temperature ionic liquid (IL), which can find useful application for analysis in hydrophobic matrices. The method, developed here for the case of lead ions, is based on the galvanostatic dissolution of a lead anode dipped directly in a suitable IL, namely tri-hexyl(tetradecyl)phosphonium bis (trifluoromethylsulfonyl) imide ([P][NTf]). After each oxidation step, the metal dissolution process in the IL solutions was monitored by cyclic voltammetric measurements at a glassy carbon disk electrode. The results indicated that the peak current relevant to the reduction of the electro-generated Pb(II) increased linearly while increasing the oxidation time. By varying the oxidation time from 200 to 6000s, a set of Pb/[P][NTf] solutions at concentrations ranging between 10 and 300μgg was prepared. To validate the efficiency of the electrochemical procedure to produce metal ion standard solutions, the Pb content was quantified by developing a microwave digestion procedure specifically suitable for the IL medium, followed by ICP-QMS analysis in the digested standards. The results indicated a satisfactory agreement between concentrations found by ICP-QMS and calculated from electrochemical data, with a coulometric efficiency of Pb(II) generation in ionic liquid ≥95.6%. Finally, the applicability of the Pb/IL solutions as standards for analyses in hydrophobic media was tested by determining, by ICP-QMS, the Pb content in an extra-virgin olive oil spiked with known amounts of a Pb/IL standard. Satisfactory Pb recoveries, ≥96%, were measured.
本文提出了一种在室温离子液体(IL)中制备金属离子标准溶液的电化学方法,该方法在疏水性基质分析中可能有有用的应用。该方法是针对铅离子开发的,其原理是直接将铅阳极浸入适当的 IL(即三己基(十四烷基)膦双(三氟甲磺酰基)亚胺[P][NTf])中进行恒电流溶解。在每个氧化步骤之后,通过在玻碳圆盘电极上进行循环伏安测量来监测 IL 溶液中的金属溶解过程。结果表明,与电生成的 Pb(II)还原相关的峰电流随着氧化时间的增加而线性增加。通过将氧化时间从 200 秒变化到 6000 秒,可以制备一系列浓度在 10 到 300μg g 之间的 Pb/[P][NTf]溶液。为了验证电化学程序制备金属离子标准溶液的效率,通过专门适用于 IL 介质的微波消解程序定量 Pb 含量,然后在消解的标准品中进行 ICP-QMS 分析。结果表明,ICP-QMS 分析得到的浓度与电化学数据计算得到的浓度之间存在令人满意的一致性,Pb(II)在离子液体中的电生成效率≥95.6%。最后,通过 ICP-QMS 测定含已知量 Pb/IL 标准品的特级初榨橄榄油中的 Pb 含量,测试了 Pb/IL 溶液作为疏水性介质分析标准的适用性。测量得到了令人满意的 Pb 回收率,≥96%。